期刊
JOURNAL OF NUCLEAR MEDICINE
卷 62, 期 3, 页码 418-421出版社
SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.120.243949
关键词
synaptic vesicle protein 2A; SV2A; PET; SUVR; brain imaging
资金
- Nancy Taylor Foundation [R01NS094253, R01AG052560, R01MH104459]
This study compared SUVR-1 with BPND to select the optimal time window in healthy and neuropsychiatric subjects, finding that SUVR-1 showed greater correlation and less bias at later time windows. The 60-90 min period provided the best match between SUVR-1 and BPND.
C-11-UCB-J ((R)-1-((3-(C-11-methyl-C-11)pyridin-4-yl)-methyl)-4-(3,4,5-trifluorophenyl)pyrrolidin-2-one) is a PET tracer for synaptic vesicle glycoprotein 2A, which may be a marker of synaptic density. To simplify the scan protocol, SUV ratios (SUVRs) were compared with model-based nondisplaceable binding potential (BPND) to select the optimal time window in healthy and neuropsychiatric subjects. Methods: In total, 141 scans were acquired for 90 min. Arterial blood sampling and metabolite analysis were conducted. SUVR-1 (centrum semiovale reference region) was computed for six 30-min windows and compared with 1-tissue-compartment model BPND. Simulations were performed to assess the time dependency of SUVR-1. Results: Greater correlation and less bias were observed for SUVR-1 at later time windows for all subjects. Simulations showed that the agreement between SUVR-1 and BPND is time-dependent. Conclusion: The 60- to 90-min period provided the best match between SUVR-1 and BPND (-1% +/- 7%); thus, a short scan is sufficient for accurate quantification of C-11-UCB-J-specific binding.
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